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Journal of Ovarian Research|April 23, 2020
Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating familyQiong Xing, Ruyi Wang, Beili Chen, et al.Frontiers in Cardiovascular Medicine|July 25, 2022
Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of MYOM2Jing Wang, Chunyan Wang, Haiyang Xie, et al.Reproductive Biomedicine Online|November 25, 2017
A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiencyWei Zhang, Jing Wang, Xi Wang, et al.Systems Biology in Reproductive Medicine|May 15, 2025
Novel homozygous missense variants in SUN5 and DNAH10 associated with male infertility and oligoasthenoteratozoospermiaQi Fang, Lanxi Ran, Xinying Bi, et al.Journal of Human Genetics|April 29, 2016
Claudin-7 indirectly regulates the integrin/FAK signaling pathway in human colon cancer tissueLei Ding, Liyong Wang, Leiming Sui, et al.The American Journal of Pathology|October 20, 2018
CAPS Mutations Are Potentially Associated with Unexplained Recurrent Pregnancy LossHong Pan, Huifen Xiang, Jing Wang, et al.Fertility and Sterility|July 9, 2019
Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiencyYiran Zhou, Beili Chen, Lin Li, et al.Genetic Testing and Molecular Biomarkers|June 5, 2024
Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like PhenotypesZhonglin Liu, Chunyan Wang, Feng Ni, et al.Human Reproduction (Oxford, England)|September 24, 2017
Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicingBinbin Wang, Lin Li, Ying Zhu, et al.Frontiers in Genetics|December 20, 2021
Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese CohortHuifen Xiang, Chunyan Wang, Hong Pan, et al.Pageof 4